HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → HCID 59612107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 5-Hexenoic acid, 6-[p-chlorophenyl]-2,4-dioxo-, ethyl ester | HCID 5375825 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59612107 | HCID 59612107 | 86% |
Reaction Steps
Using the procedure of Example 4, (E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid ethyl ester (4; 79.5 g, 0.284 mol) and ammonium acetate (43.78 g, 0.568 mol) were allowed to react in EtOH (795 mL) to provide (2Z,5E)-2-amino-6-(4-chlorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester (8; 47 g, 86%) as a yellow solid: mp 105-107° C.; 1H NMR (400 MHz, CDCl3) δ 9.40 (br s, 1H), 7.52 (d, J=15.9 Hz, 1H), 7.50-7.47 (m, 2H), 7.38-7.32 (m, 2H), 6.78 (d, J=15.9 Hz, 1H), 6.14 (s, 1H), 6.01 (s, 1H), 4.37 (q, J=7.1 Hz, 2H), 1.39 (t, J=7.1 Hz, 3H); HRMS-ESI (m/z): calcd for C14H14ClNO3, 279.067. found, 279.066.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08252938B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-15e48261282d435887b503dba8e9adc6 |
| Source note | uspto-grants-2012_08 |